RT Journal Article
SR Electronic
T1 Relationship between amyloid and tau levels and its impact on tau spreading
JF Journal of Nuclear Medicine
JO J Nucl Med
FD Society of Nuclear Medicine
SP 116
OP 116
VO 62
IS supplement 1
A1 Dore, Vincent
A1 Krishnadas, Natasha
A1 Bourgeat, Pierrick
A1 Huang, Kun
A1 Li, Shenpeng
A1 Burnham, Samantha
A1 Masters, Colin
A1 Fripp, Jurgen
A1 Villemagne, Victor
A1 Rowe, Christopher
YR 2021
UL http://jnm.snmjournals.org/content/62/supplement_1/116.abstract
AB 116Purpose: Previous studies have shown that Aβ-amyloid (Aβ) likely promotes tau to spread beyond the medial temporal lobe. However, the Aβ levels necessary for tau to spread in the neocortex is still unclear. Methods: 466 participants underwent tau imaging with [18F]MK6420 and Aβ imaging with [18F]NAV4694. Aβ scans were quantified on the Centiloid (CL) scale with a cut-off of 25CL for abnormal levels of Aβ (A+). Tau scans were quantified in three regions of interest (ROI) (mesial temporal (Me); temporoparietal neocortex (Te); and rest of neocortex (R)) and four mesial temporal region (entorhinal cortex, amygdala, hippocampus and parahippocampus) using the cerebellar cortex as reference region. Regional tau thresholds were established as the 95%ile of the cognitively unimpaired A- subjects. The prevalence of abnormal tau levels (T+) along the Centiloid continuum was determined. Results: The plots of prevalence of T+ show earlier and greater increase along the Centiloid continuum in the medial temporal area compared to neocortex. Prevalence of T+ was low but associated with Aβ level between 10-40 CL reaching 23% in Me, 15% in Te and 11% in R. Between 40-70 CL, the prevalence of T+ subjects per CL increased four-fold faster and at 70 CL was 64% in Me, 51% in Te and 37% in R. In cognitively unimpaired, there were no T+ in R below 50 CL. The highest prevalence of T+ was found in the entorhinal cortex, reaching 40% at 40 CL and 80% at 60 CL. Conclusions: Outside the entorhinal cortex, abnormal levels of cortical tau on PET are rarely found with Aβ levels below 40 CL. Above 40 CL prevalence of T+ accelerates in all areas. Moderate Aβ levels are required before neocortical tau becomes detectable.